IF 9.7 1区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Yen Lin Chu, Peter Georgeson, Mark Clendenning, Khalid Mahmood, Romy Walker, Julia Como, Sharelle Joseland, Susan G Preston, Toni Rice, Brigid M Lynch, Roger L Milne, Melissa C Southey, Graham G Giles, Amanda I Phipps, John L Hopper, Aung K Win, Christophe Rosty, Finlay A Macrae, Ingrid Winship, Mark A Jenkins, Daniel D Buchanan, Jihoon E Joo
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引用次数: 0

摘要

背景:林奇综合征(Lynch Syndrome,LS)患者罹患结直肠癌(CRC)和并发 CRC 的风险存在差异,这可能与肠道微生物群的不良影响有关。pks+/-大肠埃希氏菌(pks+/-E. coli)、肠毒性脆弱拟杆菌(ETBF)和核酸镰刀菌(Fn)在林奇综合征患者的结直肠癌和腺瘤中的作用尚不清楚:方法:使用多重 TaqMan qPCR 对澳大利亚结肠癌家族登记处的 358 例 LS 病例(包括 386 例 CRC、90 例腺瘤和 195 例正常结肠粘膜 DNA)进行了检测。使用 Logistic 回归比较了林奇型结肠癌与 1336 例散发性结肠癌中每种细菌的瘤内流行率。Cox 比例危险度回归估算了每种细菌与远期 CRC 和肿瘤风险的相关性:Pks+大肠杆菌(几率比[95%置信区间] = 1.60 [1.08-2.35],P = 0.017)、pks-大肠杆菌(3.87 [2.58-5.80],P +初始 CRC 中的大肠杆菌与远期 CRC 风险增加有关(危险比[95%置信区间] = 2.32 [1.29-4.17],P = 0.005)和变异性结直肠肿瘤(1.51 [1.02-2.23],P = 0.040)相关:Pks+大肠杆菌、pks-E. coli和Fn在LS型CRC中富集,表明它们可能在LS型CRC的发展中发挥作用。瘤内pks+大肠杆菌与罹患远期CRC的风险增加有关,这表明如果得到验证,LS患者可能会从pks+大肠杆菌筛查和根除中获益:本研究由NHMRC研究者基金(GNT1194896)和澳大利亚癌症协会/新南威尔士州癌症理事会联合基金(GNT2012914)资助。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intratumoural pks+Escherichia coli is associated with risk of metachronous colorectal cancer and adenoma development in people with Lynch syndrome.

Background: The adverse gut microbiome may underlie the variability in risks of colorectal cancer (CRC) and metachronous CRC in people with Lynch syndrome (LS). The role of pks+/-Escherichia coli (pks+/-E. coli), Enterotoxigenic Bacteroides fragilis (ETBF), and Fusobacterium nucleatum (Fn) in CRCs and adenomas in people with LS is unknown.

Methods: A total of 358 LS cases, including 386 CRCs, 90 adenomas, 195 normal colonic mucosa DNA from the Australasian Colon Cancer Family Registry were tested using multiplex TaqMan qPCR. Logistic regression was used to compare the intratumoural prevalence of each bacteria in Lynch CRCs with 1336 sporadic CRCs. Cox proportional-hazards regression estimated the associations of each bacteria with the risk of metachronous CRC and neoplasia.

Findings: Pks+ E. coli (odds ratio [95% confidence interval] = 1.60 [1.08-2.35], P = 0.017), pks-E. coli (3.87 [2.58-5.80], P < 0.001) and Fn (19.47 [13.32-28.87], P < 0.001) were significantly enriched in LS CRCs when compared with sporadic CRCs. Pks+ E. coli in the initial CRC was associated with an increased risk of metachronous CRC (hazard ratio [95% confidence interval] = 2.32 [1.29-4.17], P = 0.005) and metachronous colorectal neoplasia (1.51 [1.02-2.23], P = 0.040) when compared with CRCs without pks+ E. coli.

Interpretation: Pks+ E. coli, pks-E. coli, and Fn are enriched within LS CRCs, suggesting possible roles in CRC development in LS. Having intratumoural pks+ E. coli is associated with increased risk of metachronous CRC, suggesting that, if validated, people with LS might benefit from pks+ E. coli screening and eradication.

Funding: This work was funded by an NHMRC Investigator grant (GNT1194896) and a Cancer Australia/Cancer Council NSW co-funded grant (GNT2012914).

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来源期刊
EBioMedicine
EBioMedicine Biochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
CiteScore
17.70
自引率
0.90%
发文量
579
审稿时长
5 weeks
期刊介绍: eBioMedicine is a comprehensive biomedical research journal that covers a wide range of studies that are relevant to human health. Our focus is on original research that explores the fundamental factors influencing human health and disease, including the discovery of new therapeutic targets and treatments, the identification of biomarkers and diagnostic tools, and the investigation and modification of disease pathways and mechanisms. We welcome studies from any biomedical discipline that contribute to our understanding of disease and aim to improve human health.
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